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Mendeliome

Gene: ALOX12

Red List (low evidence)

ALOX12 (arachidonate 12-lipoxygenase, 12S type)
EnsemblGeneIds (GRCh38): ENSG00000108839
EnsemblGeneIds (GRCh37): ENSG00000108839
OMIM: 152391, Gene2Phenotype
ALOX12 is in 1 panel

1 review

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Red List (low evidence)

Cannot find association with Mendelian disease.
Created: 14 Jul 2020, 12:05 a.m. | Last Modified: 14 Jul 2020, 12:05 a.m.
Panel Version: 0.3313

Details

Mode of Inheritance
Unknown
Sources
  • Expert Review Red
  • Victorian Clinical Genetics Services
OMIM
152391
Clinvar variants
Variants in ALOX12
Penetrance
None
Panels with this gene

History Filter Activity

14 Jul 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: alox12 has been classified as Red List (Low Evidence).

14 Jul 2020, Gel status: 1

Entity classified by Genomics England curator

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

Gene: alox12 has been classified as Red List (Low Evidence).

17 Nov 2019, Gel status: 3

Created, Added New Source, Set mode of inheritance

Zornitza Stark (Victorian Clinical Genetics Services; Australian Genomics)

gene: ALOX12 was added gene: ALOX12 was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: ALOX12 was set to Unknown